On Thursday, The Patriot Daily Wire reported that the Food and Drug Administration (FDA) has released more information about the possible side effects of the Pfizer coronavirus vaccine.

The article reports:

As the FDA prepares to approve Pfizer’s new pill for treating high-risk patients infected with COVID, more information about dangerous side effects tied to its vaccine are coming to light.

Just yesterday, we reported another death tied to the vaccine in New Zealand. Now, documents released by the FDA reveal that drugmaker Pfizer recorded nearly 160K adverse reactions to its COVID vaccine in the initial months of its rollout.

The data were obtained by a group of doctors, professors, and journalists calling themselves Public Health and Medical Professionals for Transparency. They filed a Freedom of Information Act request with the FDA asking for their release. And the first tranche of documents revealed that, as of February 2021, when Pfizer’s shot was being rolled out worldwide on an emergency basis, the drugmaker had compiled more than 42K case reports detailing nearly 160K individual adverse reactions to the vaccine.

The data show the bulk of the adverse event cases, both serious and non-serious, were classified as “general disorders”.

You shouldn’t have to file a Freedom of Information request to get this data–it should be given to everyone who is considering getting the vaccine.

Please follow the link above to read the entire article. It includes the complete breakdown of data from Public Health and Medical Professionals For Transparency. There has to be a risk/benefit analysis when considering getting the vaccine. There also needs to be a discussion about how effective the vaccine actually is.